Centurion Medical recalls CVC TRIPLE LUMEN SAFETY BUNDLE ECVC6070 due to potential fluid droplets separating after disconnection. Affected units sold in 2018.
Firm distributes kits which include the BD MaxZeroNeedleess Connector, which was recalled by the manufacturer due to the potential for droplets of fluid separating from the sealed surface of the connector following disconnection.
Centurion Medical is recalling a specific CVC triple lumen safety bundle (ECVC6070) because fluid droplets might separate from the connector after it's disconnected. This could lead to contamination or infection risks during medical procedures.
The BD MaxZeroNeedleless Connector in the bundle may release fluid droplets when disconnected. This could cause contamination or infection if the droplets come into contact with the patient or medical equipment.
Healthcare professionals using this bundle for central venous catheter procedures are most at risk. Patients receiving treatments through this equipment could also be affected.
Check for the model ECVC6070 on the bundle packaging. Units were sold starting in 2018 with serial numbers 2018081550, 2018091750, and 2018100850.
Look for the model ECVC6070 on the bundle packaging or check the serial numbers 2018081550, 2018091750, or 2018100850.
The product is not safe to use as it poses a risk of fluid droplets separating after disconnection, which could lead to contamination.
Check for the model ECVC6070 on the bundle packaging or look for the serial numbers 2018081550, 2018091750, or 2018100850.
The recall record does not specify a remedy, so contact Centurion Medical directly for guidance.
We’ve drafted a message you can send Centurion Medical to request your refund or repair — edit it as you like.
Subject: Recall Z-0095-2020 — Centurion Medical Centurion Medical Hello, I own a Centurion Medical that is covered by recall Z-0095-2020 from Centurion Medical. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
